Asymmetric synthesis of homochiral Baylis-Hillman products employing (R)-N-methyl-N-alpha-methylbenzyl amide

The conjugate addition of (R)-N-methyl-N-α-methylbenzyl amide to tert-butyl cinnamate followed by an asymmetric aldol reaction and subsequent N-oxidation/Cope elimination affords β-substituted homochiral Baylis-Hillman products in good yield. Copyright (C) 2000 Elsevier Science Ltd.

গ্রন্থ-পঞ্জীর বিবরন
প্রধান লেখক: Davies, S, Smethurst, C, Smith, A, Smyth, G
বিন্যাস: Journal article
ভাষা:English
প্রকাশিত: 2000
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author Davies, S
Smethurst, C
Smith, A
Smyth, G
author_facet Davies, S
Smethurst, C
Smith, A
Smyth, G
author_sort Davies, S
collection OXFORD
description The conjugate addition of (R)-N-methyl-N-α-methylbenzyl amide to tert-butyl cinnamate followed by an asymmetric aldol reaction and subsequent N-oxidation/Cope elimination affords β-substituted homochiral Baylis-Hillman products in good yield. Copyright (C) 2000 Elsevier Science Ltd.
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spelling oxford-uuid:40ea594a-0f7d-43d2-9ab1-1cbe1612b5cb2022-03-26T14:40:37ZAsymmetric synthesis of homochiral Baylis-Hillman products employing (R)-N-methyl-N-alpha-methylbenzyl amideJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:40ea594a-0f7d-43d2-9ab1-1cbe1612b5cbEnglishSymplectic Elements at Oxford2000Davies, SSmethurst, CSmith, ASmyth, GThe conjugate addition of (R)-N-methyl-N-α-methylbenzyl amide to tert-butyl cinnamate followed by an asymmetric aldol reaction and subsequent N-oxidation/Cope elimination affords β-substituted homochiral Baylis-Hillman products in good yield. Copyright (C) 2000 Elsevier Science Ltd.
spellingShingle Davies, S
Smethurst, C
Smith, A
Smyth, G
Asymmetric synthesis of homochiral Baylis-Hillman products employing (R)-N-methyl-N-alpha-methylbenzyl amide
title Asymmetric synthesis of homochiral Baylis-Hillman products employing (R)-N-methyl-N-alpha-methylbenzyl amide
title_full Asymmetric synthesis of homochiral Baylis-Hillman products employing (R)-N-methyl-N-alpha-methylbenzyl amide
title_fullStr Asymmetric synthesis of homochiral Baylis-Hillman products employing (R)-N-methyl-N-alpha-methylbenzyl amide
title_full_unstemmed Asymmetric synthesis of homochiral Baylis-Hillman products employing (R)-N-methyl-N-alpha-methylbenzyl amide
title_short Asymmetric synthesis of homochiral Baylis-Hillman products employing (R)-N-methyl-N-alpha-methylbenzyl amide
title_sort asymmetric synthesis of homochiral baylis hillman products employing r n methyl n alpha methylbenzyl amide
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AT smitha asymmetricsynthesisofhomochiralbaylishillmanproductsemployingrnmethylnalphamethylbenzylamide
AT smythg asymmetricsynthesisofhomochiralbaylishillmanproductsemployingrnmethylnalphamethylbenzylamide